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Collapse of the native structure caused by a single amino acid exchange in human NAD(P)H:quinone oxidoreductase(1.)Fluorescent materials for pH sensing and imaging based on novel 1,4-diketopyrrolo-[3,4-c]pyrrole dyes†Electronic supplementary information (ESI) available: NMR and MS spectra, further sensor characteristics and sensor long-time performance. See DOI:Thin organic films by atmospheric-pressure ion deposition.Fluorous iminoalditols: a new family of glycosidase inhibitors and pharmacological chaperones.New derivatives of 7-chloroquinolin-4-amine with antiprotozoal activity.The antiprotozoal potencies of newly prepared 3-azabicyclo[3.2.2]nonanes.Antiprotozoal activity of bicycles featuring a dimethylamino group at their bridgehead.New derivatives of quinoline-4-carboxylic acid with antiplasmodial activity.Antiprotozoal activity of bicyclic diamines with a N-methylpiperazinyl group at the bridgehead atom.Synthesis of 3-azabicyclo[3.2.2]nonanes and their antiprotozoal activities.1-Deoxy-D-galactonojirimycins with dansyl capped N-substituents as β-galactosidase inhibitors and potential probes for GM1 gangliosidosis affected cell lines.Alkyl and dialkylaminoethyl derivatives of 5-amino-2-azabicyclo[3.2.2]nonanes and their antiplasmodial and antitrypanosomal activities.Exceptional Oxygen Sensing Properties of New Blue Light-Excitable Highly Luminescent Europium(III) and Gadolinium(III) ComplexesHalide exchanged Hoveyda-type complexes in olefin metathesisCovalent adduct formation between the plasmalogen-derived modification product 2-chlorohexadecanal and phloretin.New fluorescent pH sensors based on covalently linkable PET rhodamines.Antiprotozoal activities of new bicyclo[2.2.2]octan-2-imines and esters of bicyclo[2.2.2]octan-2-ols.New N-methylpiperazinyl derivatives of bicyclic antiprotozoal compounds.Enhancing photoinduced electron transfer efficiency of fluorescent pH-probes with halogenated phenols.Antiplasmodial and antitrypanosomal activities of aminobicyclo[2.2.2]octyl omega-aminoalkanoates.Synthesis of bicyclic amines and their activities against Trypanosoma brucei rhodesiense and Plasmodium falciparum K1.Novel azabicyclo[3.2.2]nonane derivatives and their activities against Plasmodium falciparum K1 and Trypanosoma brucei rhodesiense.Bicyclo[2.2.2]octyl esters of dialkylamino acids as antiprotozoals.Antiprotozoal activities of new bis-chlorophenyl derivatives of bicyclic octanes and aza-nonanes.Highly photostable near-infrared fluorescent pH indicators and sensors based on BF2-chelated tetraarylazadipyrromethene dyes3β-Hydroxy-28-norolea-12,17-dien-11-one.Stable Silenolates and Brook-Type Silenes with Exocyclic Structures1,3-Diphenyl-3,4-dihydro-benzo[b][1,6]naphthyridine.Tunable phosphorescent NIR oxygen indicators based on mixed benzo- and naphthoporphyrin complexes.Strongly Phosphorescent Iridium(III)-Porphyrins - New Oxygen Indicators with Tuneable Photophysical Properties and Functionalities.Derivatives of schisandrin with increased inhibitory potential on prostaglandin E(2) and leukotriene B(4) formation in vitro.Cycloartane triterpenes from dikamali, the gum resin of Gardenia gummifera and Gardenia lucida.Fluorescent organophosphonates as inhibitors of microbial lipases.Inverse electron demand Diels-Alder (iEDDA) functionalisation of macroporous poly(dicyclopentadiene) foams.Novel fluorescent phosphonic acid esters for discrimination of lipases and esterases.Investigation of primary crystallite sizes in nanocrystalline ZnS powders: comparison of microwave assisted with conventional synthesis routes.Investigations on the formation of 4-aminobicyclo[2.2.2]-octanones.Epimers of bicyclo[2.2.2]octan-2-ol derivatives with antiprotozoal activity.Synthesis of new 1-benzyl tetrahydropyridinylidene ammonium salts and their antimicrobial and anticellular activities.Synthesis and properties of new phosphorescent red light-excitable platinum(II) and palladium(II) complexes with Schiff bases for oxygen sensing and triplet-triplet annihilation-based upconversion.
P50
Q24302315-4CF54A2C-9DCC-49E9-B561-1C46F42D684BQ30670711-682398C6-96E1-4E6B-AD73-D9B5D83A6C27Q33431510-5FCDFF8E-1017-4237-986F-557AA9FC553DQ33660528-B1754FD7-1DE4-4C56-9677-ED32FF0192D1Q38723951-4F5F32D4-FBCC-4DA8-A14F-897D17424D54Q38863176-73D82B4B-C59A-4243-BE3C-9BA6FBEFB45BQ38997966-32BEC254-9648-48DD-B797-C3FDF72DA136Q39069647-1D41E244-33B0-485D-8C54-F7F7B5665794Q39121293-6AFD66E3-6C46-4DC0-9DC3-8F33E9114347Q39443397-6049CCB2-0384-40A5-B6A5-A1D1837C9359Q39529765-8D3D5462-8E1B-40BB-9156-8671AAF1305EQ39781048-B8E27E2B-5B78-4031-B193-B8F0AE9E8446Q40938419-2BA571F7-61BE-44DD-B25D-5C85DDAFFD28Q41156828-EB5DE2D9-4068-41E6-BD87-90E8F5E3C34FQ41598092-C531158A-0B22-457A-83CC-F8531C212063Q41627895-67E480CE-FD48-48D9-9817-BD793FCCB52DQ41912646-16BD303A-552B-4293-8A68-233ACE73F13DQ41931039-7BB00321-A1D7-4E11-B0E8-83E756BA36E1Q41938053-5BB57820-2216-4E89-9995-75A2E9C36DA0Q41940730-47AE36EC-0B73-4D2F-B700-56037F0431D6Q41940763-7FD21677-D146-43CA-A433-C0AB597B17A8Q41940883-CF3C6044-C6F2-455D-9B6B-E6F967BB83B3Q41942916-29266CDA-7EF8-4A6B-9D52-86AFDC431D1CQ41944799-B877B07F-818D-4B12-8514-8616D1C050EBQ41967051-508EAF7F-70FB-48AD-B0F0-56D0ACB0CF9AQ42141224-7481D34B-C061-45B1-8189-8E0A9331B70BQ42157793-0B88C998-5BB8-489F-87F1-97E5C34A8CECQ42368853-A1D96E22-0422-4EB9-A8E4-7AD4FDA3D3FDQ42410969-C866BD11-1064-4D92-A2F6-CCF2390CAF58Q42558529-01034C7F-BC49-458E-BAF4-25972673FF49Q43126037-F279386D-E85A-4296-AF50-ABB9B0A122C2Q43288283-D2E702AD-FECD-4E9C-B27F-18E9F7A214D4Q44589997-6823E03D-C003-4595-AF6A-ABF896C437C4Q45338068-44AACD88-16F7-420C-A4B1-2565390656C9Q46645330-87921C70-6630-4ECA-9998-83A24BD46D45Q46693172-A9361535-7EA2-4DA1-B7F6-4E5A1BA2846AQ46897167-698C167C-413A-4B17-8BCF-C81357C2D3C9Q47840584-46D77D5F-FAE2-4B9C-AE58-F3396A3BCD83Q49677702-2E2B5743-4053-4A25-97C9-4D36309F2140Q50499021-474120B5-9834-451F-B45F-EB6072956D04
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Robert Saf
@ast
Robert Saf
@en
Robert Saf
@es
Robert Saf
@nl
Robert Saf
@sl
type
label
Robert Saf
@ast
Robert Saf
@en
Robert Saf
@es
Robert Saf
@nl
Robert Saf
@sl
prefLabel
Robert Saf
@ast
Robert Saf
@en
Robert Saf
@es
Robert Saf
@nl
Robert Saf
@sl
P1053
O-9061-2016
P106
P21
P31
P3829
P496
0000-0003-3858-6193